Results 81 to 90 of about 10,393 (275)
A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemia [PDF]
, 2017 NDUFB11, a component of mitochondrial complex I, is a relatively small integral membrane protein, belonging to the 'supernumerary' group of subunits, but proved to be absolutely essential for the assembly of an active complex I.
Bertini, Enrico +21 more
core +2 more sources
Journal of Family Medicine and Primary Care, 2019 Background: In developing world, anemia is a significant cause of mortality and morbidity in children under 5 years of age. Iron deficiency anemia (IDA) is a very important causative factor for childhood anemia.
Dipshikha Maiti +2 more
doaj +1 more source
Portable system for the prediction of anemia based on the ocular conjunctiva using Artificial Intelligence [PDF]
arXiv, 2019 Anemia is a major health burden worldwide. Examining the hemoglobin level of blood is an important way to achieve the diagnosis of anemia, but it requires blood drawing and a blood test. In this work we propose a non-invasive, fast, and cost-effective screening test for iron-deficiency anemia in Peruvian young children.
arxiv
Hashimoto's thyroiditis and autoimmune gastritis [PDF]
, 2017 The term "thyrogastric syndrome" defines the association between autoimmune thyroid disease and chronic autoimmune gastritis (CAG), and it was first described in the early 1960s.
Brusca, Nunzia +6 more
core +3 more sources
Macrocytosis is highly prevalent in Raebareli district, Uttar Pradesh, India [PDF]
, 2020 Background: Anemia is a most common health issue in Indian population mainly due to nutritional deficiencies. A number of factors contribute in anemia which is further categorized based on various parameters in hematological indices and microscopic ...
Gani, Mohd. Usman +2 more
core +2 more sources
Cancer Medicine, 2020 Large granular lymphocyte (LGL) leukemia is a rare hematological disorder with expansion of the T‐cell or natural killer (NK) cell lineage. Signal transducer and activator of transcription 3 (STAT3) exhibits somatic activating mutations in 30%‐40% of LGL
Kristine C. Olson +8 more
doaj +1 more source
Diagnosis of sickle cell anemia using AutoML on UV-Vis absorbance spectroscopy data [PDF]
arXiv, 2021 Sickle cell anemia is a genetic disorder that is widespread in many regions of the world. Early diagnosis through screening and preventive treatments are known to reduce mortality in the case of sickle cell disease (SCD). In addition, the screening of individuals with the largely asymptomatic condition of sickle cell trait (SCT) is necessary to curtail
arxiv
Novel Meta-Heuristic Model for Discrimination between Iron Deficiency Anemia and B-Thalassemia with CBC Indices Based on Dynamic Harmony Search [PDF]
arXiv, 2020 In recent decades, attention has been directed at anemia classification for various medical purposes, such as thalassemia screening and predicting iron deficiency anemia (IDA). In this study, a new method has been successfully tested for discrimination between IDA and \b{eta}-thalassemia trait (\b{eta}-TT).
arxiv